Covidien Llc: Stethoscope, Esophageal, With Electrical Conductors
Recall Summary Covidien LLC is recalling Mon-a-Therm General Purpose Temperature Probes (model 90044) that were distributed nationwide because the devices lack required FDA clearance. These esophageal temperature probes with electrical conductors were sold to healthcare facilities across the United States. The recall is classified as Class II, meaning the devices do not meet regulatory requirements for market distribution.
- Recalling firm
- Covidien LLC
- Product
- Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
- Reason
- Temperature probe devices lack FDA clearance.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-04-23
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, FL, GA, HI, IL, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, WA, WV.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/56b53fd3-8a74-446c-9f52-79632cc3929f